A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434812



Internal ID21396814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164930512..164931511hg38UCSC Ensembl
chr6:165344001..165345000hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15745779, nssv15748162
SamplesMDQ010, MDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434812
Frequency
Sample Size15
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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